Regulatory Strategy Director

GEE Group; Cleveland (OH); On-site; USD 140,000 - 180,000; Full time

Job summary

GEE Group is seeking a Director of Regulatory Affairs to lead product compliance and shape regulatory strategy across markets. You will translate complex requirements into practical actions while building standardized documentation, approvals, and change controls.

You will guide teams on labeling, SDS, training, and regulatory submissions, coordinating with manufacturing, quality, and commercial groups to enable launches and market expansion.

Qualifications

• 10+ years in regulatory affairs, product stewardship, or chemical compliance.
• Strong knowledge of chemical classification, labeling, and commercialization requirements.
• Experience with OSHA, EPA, DOT, FDA, TSCA, CARB, Prop 65, REACH.

Responsibilities

• Own regulatory oversight throughout the product lifecycle from development to sale.
• Evaluate compliance implications of changes to ingredients, packaging, claims and formulas.
• Ensure labeling, safety data sheets, warnings, and technical information meet requirements.
• Monitor regulatory developments and advise leadership on impact and timelines.
• Strengthen reviews, change management, record retention and submissions processes.
• Partner with technical, manufacturing and commercial teams on launches and changes.
• Provide guidance for customer-branded products, international distribution, and online sales.
• Coordinate with EHS leadership where regulatory matters intersect with safety.
• Develop procedures and training to apply regulatory requirements consistently.
• Serve as a knowledgeable resource for customers and internal stakeholders.

Skills

Regulatory affairs

Regulatory strategy

Hazard communication

Regulatory risk assessment

Cross-functional collaboration

Education

Bachelor's degree in chemistry / chemical engineering / regulatory science

Job description

GEE Group is seeking a Director of Regulatory Affairs to lead product compliance and shape regulatory strategy across markets. You will translate complex requirements into practical actions while building standardized documentation, approvals, and change controls.

You will guide teams on labeling, SDS, training, and regulatory submissions, coordinating with manufacturing, quality, and commercial groups to enable launches and market expansion.